Incidental Mutation 'R0745:Zbbx'
ID 474135
Institutional Source Beutler Lab
Gene Symbol Zbbx
Ensembl Gene ENSMUSG00000034151
Gene Name zinc finger, B-box domain containing
Synonyms
MMRRC Submission 038926-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # R0745 (G1)
Quality Score 225
Status Not validated
Chromosome 3
Chromosomal Location 74945214-75072341 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 75062734 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 8 (V8I)
Ref Sequence ENSEMBL: ENSMUSP00000122459 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000124618]
AlphaFold Q0P5X5
Predicted Effect probably damaging
Transcript: ENSMUST00000124618
AA Change: V8I

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000122459
Gene: ENSMUSG00000034151
AA Change: V8I

DomainStartEndE-ValueType
coiled coil region 23 60 N/A INTRINSIC
Pfam:zf-B_box 128 174 1.3e-7 PFAM
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.4%
  • 20x: 95.0%
Validation Efficiency 100% (40/40)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd12 A T 2: 150,675,068 (GRCm39) probably null Het
Adam17 A G 12: 21,382,222 (GRCm39) probably benign Het
Aldh1l2 T A 10: 83,354,494 (GRCm39) probably null Het
Bltp1 A G 3: 36,982,612 (GRCm39) Y759C probably damaging Het
Brca2 A T 5: 150,468,347 (GRCm39) probably benign Het
Capn13 A C 17: 73,658,503 (GRCm39) D188E probably benign Het
Col14a1 A T 15: 55,201,813 (GRCm39) T34S unknown Het
Col5a2 A G 1: 45,446,387 (GRCm39) probably null Het
Cyp4v3 A G 8: 45,761,688 (GRCm39) probably benign Het
Dlat G A 9: 50,565,008 (GRCm39) T233M probably damaging Het
Eef2 C T 10: 81,017,830 (GRCm39) P831S probably benign Het
Endod1 A T 9: 14,268,413 (GRCm39) N357K possibly damaging Het
Evc A T 5: 37,476,403 (GRCm39) V205E probably damaging Het
Fryl A G 5: 73,228,469 (GRCm39) L1754P probably damaging Het
Gabra6 A T 11: 42,207,394 (GRCm39) M230K probably damaging Het
Hsd3b5 A G 3: 98,526,855 (GRCm39) V197A probably benign Het
Kmt2c A T 5: 25,564,696 (GRCm39) probably null Het
Mthfsd A T 8: 121,829,688 (GRCm39) L116Q probably damaging Het
Mug1 A G 6: 121,864,386 (GRCm39) T1428A probably benign Het
Obscn A G 11: 58,973,065 (GRCm39) V2312A probably benign Het
Or1i2 T C 10: 78,447,956 (GRCm39) E173G probably benign Het
Palld G A 8: 62,330,737 (GRCm39) R47C probably damaging Het
Pds5b A G 5: 150,729,136 (GRCm39) T1424A probably benign Het
Ppp6r2 G A 15: 89,149,445 (GRCm39) probably null Het
Sik3 A G 9: 46,109,537 (GRCm39) N505S probably benign Het
Spin1 A G 13: 51,293,551 (GRCm39) Y87C probably damaging Het
Tcp11 T C 17: 28,286,134 (GRCm39) I494V possibly damaging Het
Tgfa G A 6: 86,248,417 (GRCm39) E140K probably damaging Het
Trappc9 G A 15: 72,897,816 (GRCm39) R377W probably damaging Het
Trmo A G 4: 46,382,104 (GRCm39) F338L probably damaging Het
Tspan17 T C 13: 54,937,487 (GRCm39) V27A possibly damaging Het
Tut4 C G 4: 108,360,152 (GRCm39) probably benign Het
Uba5 A G 9: 103,926,710 (GRCm39) probably benign Het
Unc5a CTGTGTGTGTGTGTGT CTGTGTGTGTGTGT 13: 55,153,068 (GRCm39) probably null Het
Zfp451 A T 1: 33,809,929 (GRCm39) L931* probably null Het
Zmym4 A T 4: 126,796,496 (GRCm39) probably benign Het
Other mutations in Zbbx
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00561:Zbbx APN 3 74,968,839 (GRCm39) critical splice donor site probably null
IGL01328:Zbbx APN 3 75,000,382 (GRCm39) nonsense probably null
IGL01340:Zbbx APN 3 75,012,957 (GRCm39) missense possibly damaging 0.53
IGL01631:Zbbx APN 3 74,985,984 (GRCm39) missense probably damaging 0.99
IGL01681:Zbbx APN 3 74,959,785 (GRCm39) missense probably damaging 1.00
IGL02427:Zbbx APN 3 75,046,905 (GRCm39) missense probably benign 0.04
IGL03077:Zbbx APN 3 74,989,153 (GRCm39) missense possibly damaging 0.61
IGL03115:Zbbx APN 3 74,985,867 (GRCm39) missense probably benign 0.03
IGL03162:Zbbx APN 3 74,978,930 (GRCm39) splice site probably benign
Eland UTSW 3 74,979,019 (GRCm39) missense probably benign 0.01
PIT4480001:Zbbx UTSW 3 75,043,794 (GRCm39) missense probably damaging 1.00
PIT4495001:Zbbx UTSW 3 74,968,944 (GRCm39) missense probably damaging 1.00
R0179:Zbbx UTSW 3 74,992,869 (GRCm39) splice site probably benign
R0396:Zbbx UTSW 3 74,985,802 (GRCm39) missense possibly damaging 0.81
R0523:Zbbx UTSW 3 74,989,165 (GRCm39) missense probably benign 0.03
R0603:Zbbx UTSW 3 74,985,757 (GRCm39) missense probably benign 0.05
R0747:Zbbx UTSW 3 75,062,734 (GRCm39) missense probably damaging 1.00
R1208:Zbbx UTSW 3 74,945,299 (GRCm39) missense possibly damaging 0.94
R1208:Zbbx UTSW 3 74,945,299 (GRCm39) missense possibly damaging 0.94
R1371:Zbbx UTSW 3 74,959,784 (GRCm39) missense possibly damaging 0.58
R1769:Zbbx UTSW 3 74,990,926 (GRCm39) splice site probably benign
R1906:Zbbx UTSW 3 74,979,047 (GRCm39) missense probably damaging 1.00
R2069:Zbbx UTSW 3 74,985,719 (GRCm39) missense probably benign 0.01
R2165:Zbbx UTSW 3 75,019,414 (GRCm39) missense probably damaging 0.99
R2174:Zbbx UTSW 3 74,959,721 (GRCm39) missense possibly damaging 0.93
R2979:Zbbx UTSW 3 74,985,793 (GRCm39) nonsense probably null
R3121:Zbbx UTSW 3 74,989,153 (GRCm39) missense possibly damaging 0.88
R3755:Zbbx UTSW 3 75,012,978 (GRCm39) missense probably damaging 1.00
R3756:Zbbx UTSW 3 75,012,978 (GRCm39) missense probably damaging 1.00
R3816:Zbbx UTSW 3 74,992,802 (GRCm39) missense probably benign 0.00
R4002:Zbbx UTSW 3 75,012,978 (GRCm39) missense probably damaging 1.00
R4003:Zbbx UTSW 3 75,012,978 (GRCm39) missense probably damaging 1.00
R4057:Zbbx UTSW 3 75,012,978 (GRCm39) missense probably damaging 1.00
R4072:Zbbx UTSW 3 75,012,978 (GRCm39) missense probably damaging 1.00
R4073:Zbbx UTSW 3 75,012,978 (GRCm39) missense probably damaging 1.00
R4075:Zbbx UTSW 3 75,012,978 (GRCm39) missense probably damaging 1.00
R4114:Zbbx UTSW 3 75,046,905 (GRCm39) missense probably benign 0.04
R4784:Zbbx UTSW 3 74,992,348 (GRCm39) missense probably benign 0.05
R4821:Zbbx UTSW 3 74,989,054 (GRCm39) missense possibly damaging 0.68
R5008:Zbbx UTSW 3 75,058,755 (GRCm39) missense possibly damaging 0.62
R5030:Zbbx UTSW 3 74,990,990 (GRCm39) missense possibly damaging 0.83
R5388:Zbbx UTSW 3 74,990,977 (GRCm39) missense probably damaging 0.98
R6398:Zbbx UTSW 3 74,985,872 (GRCm39) missense probably damaging 0.96
R6462:Zbbx UTSW 3 74,985,966 (GRCm39) missense probably benign 0.07
R6597:Zbbx UTSW 3 75,043,761 (GRCm39) missense probably damaging 1.00
R6882:Zbbx UTSW 3 74,979,019 (GRCm39) missense probably benign 0.01
R7084:Zbbx UTSW 3 75,046,853 (GRCm39) missense possibly damaging 0.92
R7096:Zbbx UTSW 3 74,989,044 (GRCm39) missense probably benign 0.03
R7102:Zbbx UTSW 3 75,019,401 (GRCm39) missense probably benign 0.06
R7256:Zbbx UTSW 3 74,947,205 (GRCm39) missense probably benign 0.02
R7537:Zbbx UTSW 3 74,992,826 (GRCm39) missense probably damaging 1.00
R7836:Zbbx UTSW 3 74,985,781 (GRCm39) missense possibly damaging 0.65
R7905:Zbbx UTSW 3 74,992,820 (GRCm39) missense probably benign 0.23
R8110:Zbbx UTSW 3 75,062,749 (GRCm39) missense possibly damaging 0.58
R8367:Zbbx UTSW 3 74,989,034 (GRCm39) critical splice donor site probably null
R8772:Zbbx UTSW 3 75,062,692 (GRCm39) missense probably benign 0.37
R8859:Zbbx UTSW 3 74,968,741 (GRCm39) missense unknown
R9012:Zbbx UTSW 3 74,968,960 (GRCm39) missense possibly damaging 0.73
R9062:Zbbx UTSW 3 74,989,124 (GRCm39) missense possibly damaging 0.78
R9119:Zbbx UTSW 3 74,985,897 (GRCm39) missense probably damaging 0.99
R9401:Zbbx UTSW 3 75,019,390 (GRCm39) missense probably benign 0.26
R9531:Zbbx UTSW 3 74,985,865 (GRCm39) missense probably damaging 1.00
R9678:Zbbx UTSW 3 75,046,841 (GRCm39) missense probably damaging 1.00
R9736:Zbbx UTSW 3 74,968,741 (GRCm39) missense unknown
R9780:Zbbx UTSW 3 74,945,359 (GRCm39) missense probably damaging 1.00
Z1177:Zbbx UTSW 3 75,012,991 (GRCm39) missense probably damaging 0.98
Z1177:Zbbx UTSW 3 74,979,090 (GRCm39) critical splice acceptor site probably null
Predicted Primers
Posted On 2017-04-14